Home News About Us Contact Contributors Disclaimer Privacy Policy Help FAQ

Home
Search
Quick Search
Advanced
Fulltext
Browse
Collections
Persons
My eDoc
Session History
Login
Name:
Password:
Documentation
Help
Support Wiki
Direct access to
document ID:


          Display Documents


Institute:
Collection:
Print in Citation style Print version     Display:
Sort by: Display records with Fulltext only
Entries: 1-8  
 Basket 
A dual role of linker histone H1.4 Lys 34 acetylation in transcriptional activation
Authors: Kamieniarz, K.; Izzo, A.; Dundr, M.; Tropberger, P.; Ozretic, L.; Kirfel, J.; Scheer, E.; Tropel, P.; Wisniewski, J. R.; Tora, L.; Viville, S.; Buettner, R.; Schneider, R.
Date of Publication (YYYY-MM-DD): 2012-04-15
Title of Journal: Genes & Development
Volume: 26
Issue / Number: 8
Start Page: 797
End Page: 802
Document Type: Article
ID: 609824.0
AP-2 delta Is a Crucial Transcriptional Regulator of the Posterior Midbrain
Authors: Hesse, K.; Vaupel, K.; Kurt, S.; Buettner, R.; Kirfel, J.; Moser, M.
Date of Publication (YYYY-MM-DD): 2011-08-09
Title of Journal: PLoS ONE
Volume: 6
Issue / Number: 8
Start Page: [1]
End Page: [12]
Sequence Number of Article: e23483
Document Type: Article
ID: 572101.0
 
Full text / Content available
Cloning, expression and characterization of the murine orthologue of SBF2, the gene mutated in Charcot-Marie-Tooth disease type 4B2
Authors: Kirfel, J.; Senderek, J.; Moser, M.; Roper, A.; Stendel, C.; Bergmann, C.; Zerres, K.; Buettner, R.
Date of Publication (YYYY-MM-DD): 2006-10
Title of Journal: Gene Expression Patterns
Volume: 6
Issue / Number: 8
Start Page: 978
End Page: 984
Document Type: Article
ID: 289654.0
Diagnosis, pathogenesis, and treatment prospects in cystic kidney disease
Authors: Bergmann, C.; Frank, V.; Kupper, F.; Kamitz, D.; Hanten, J.; Berges, P.; Mager, S.; Moser, M.; Kirfel, J.; Buttner, R.; Senderek, J.; Zerres, K.
Date of Publication (YYYY-MM-DD): 2006
Title of Journal: Molecular Diagnosis & Therapy
Volume: 10
Issue / Number: 3
Start Page: 163
End Page: 174
Document Type: Article
ID: 288903.0
A mouse model for cystic biliary dysgenesis in autosomal recessive polycystic kidney disease (ARPKD)
Authors: Moser, M.; Matthiesen, S.; Kirfel, J.; Schorle, H.; Bergmann, C.; Senderek, J.; Rudnik-Schoneborn, S.; Zerres, K.; Buettner, R.
Date of Publication (YYYY-MM-DD): 2005-05
Title of Journal: Hepatology
Volume: 41
Issue / Number: 5
Start Page: 1113
End Page: 1121
Document Type: Article
ID: 254903.0
PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD)
Authors: Bergmann, C.; Senderek, J.; Küpper, F.; Schneider, F.; Dornia, C.; Windelen, E.; Eggermann, T.; Rudnik-Schöneborn, S.; Kirfel, J.; Furu, L.; Onuchic, L. E.; Rossetti, S.; Harris, P. C.; Somlo, S.; Guay-Woodford, L.; Germino, G. G.; Moser, M.; Büttner, R.; Zerres, K.
Date of Publication (YYYY-MM-DD): 2004
Title of Journal: Human Mutation
Volume: 23
Issue / Number: 5
Start Page: 453
End Page: 463
Document Type: Article
ID: 221575.0
PKHD1 mutations in families requesting prenatal diagnosis for autosomal recessive polycystic kidney disease (ARPKD)
Authors: Bergmann, C.; Senderek, J.; Schneider, F.; Dornia, C.; Kupper, F.; Eggermann, T.; Rudnik-Schöneborn, S.; Kirfel, J.; Moser, M.; Büttner, R.; Zerres, K.
Date of Publication (YYYY-MM-DD): 2004
Title of Journal: Human Mutation
Volume: 23
Issue / Number: 5
Start Page: 487
End Page: 495
Document Type: Article
ID: 221576.0
New options for prenatal diagnosis in autosomal recessive polycystic kidney disease by mutation analysis of the PKHD1 gene
Authors: Zerres, K.; Senderek, J.; Rudnik-Schoneborn, S.; Eggermann, T.; Kunze, J.; Mononen, T.; Kaariainen, H.; Kirfel, J.; Moser, M.; Buettner, R.; Bergmann, C.
Date of Publication (YYYY-MM-DD): 2004
Title of Journal: Clinical Genetics
Volume: 66
Start Page: 53
End Page: 57
Document Type: Article
ID: 226621.0
Entries: 1-8  
The scope and number of records on eDoc is subject to the collection policies defined by each institute - see "info" button in the collection browse view.